2-O-METHYL-ALPHA-D-N-ACETYLNEURAMINIC ACID

Modify Date: 2024-01-11 15:54:05

2-O-METHYL-ALPHA-D-N-ACETYLNEURAMINIC ACID Structure
2-O-METHYL-ALPHA-D-N-ACETYLNEURAMINIC ACID structure
Common Name 2-O-METHYL-ALPHA-D-N-ACETYLNEURAMINIC ACID
CAS Number 50930-22-8 Molecular Weight 323.296
Density 1.5±0.1 g/cm3 Boiling Point 732.6±60.0 °C at 760 mmHg
Molecular Formula C12H21NO9 Melting Point N/A
MSDS USA Flash Point 396.9±32.9 °C

 Names

Name (2R,4R,5R)-5-acetamido-4-hydroxy-2-methoxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]oxane-2-carboxylic acid
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.5±0.1 g/cm3
Boiling Point 732.6±60.0 °C at 760 mmHg
Molecular Formula C12H21NO9
Molecular Weight 323.296
Flash Point 396.9±32.9 °C
Exact Mass 323.121643
PSA 169.27000
LogP -2.30
Vapour Pressure 0.0±5.4 mmHg at 25°C
Index of Refraction 1.576

 Safety Information

RIDADR NONH for all modes of transport

 Articles4

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The synthesis and biological evaluation of lactose-based sialylmimetics as inhibitors of rotaviral infection.

Bioorg. Med. Chem. 14 , 739-57, (2006)

Rotaviruses are the most significant cause of gastroenteritis in young children and are responsible for over 600,000 infant deaths annually. The rotaviral haemagglutinin protein (VP8*) of some strains...

Hemagglutinins from two influenza virus variants bind to sialic acid derivatives with millimolar dissociation constants: a 500-MHz proton nuclear magnetic resonance study.

Biochemistry 28 , 8388, (1989)

The equilibrium binding of influenza virus hemagglutinin to derivatives of its cell-surface ligand, sialic acid, was measured by nuclear magnetic resonance (NMR) spectroscopy. Binding was quantified b...

Sugar-binding sites of the HA1 subcomponent of Clostridium botulinum type C progenitor toxin.

J. Mol. Biol. 376 , 854-67, (2008)

Clostridium botulinum type C 16S progenitor toxin contains a hemagglutinin (HA) subcomponent, designated HA1, which appears to play an important role in the effective internalization of the toxin in g...

 Synonyms

Methyl (6R)-5-acetamido-3,5-dideoxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]-β-L-threo-hex-2-ulopyranosidonic acid
D-glycero-α-D-galacto-2-Nonulopyranosidonic acid, methyl 5-(acetylamino)-3,5-dideoxy-
D-glycero-β-D-galacto-2-Nonulopyranosidonic acid, methyl 5-(acetylamino)-3,5-dideoxy-
2-O-Methyl-Alpha-D-N-acetylneuraminic Acid
Methyl (6R)-5-acetamido-3,5-dideoxy-6-[(1R,2R)-1,2,3-trihydroxypropyl]-α-L-threo-hex-2-ulopyranosidonic acid
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